| Tag | Content |
|---|
EnhancerAtlas ID | HS099-11220 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr19:45639670-45641360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr19:45640751-45640762 | CTGCAGCTGTT | - | 6.02 | | TP53 | MA0106.3 | chr19:45639717-45639735 | GGCATGCATGGGCTTGTC | + | 6.16 | | TP53 | MA0106.3 | chr19:45639717-45639735 | GGCATGCATGGGCTTGTC | - | 6.22 | | Tcf12 | MA0521.1 | chr19:45640751-45640762 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31565 | chr19:45641181-45642038 | Gastric | | SE_65319 | chr19:45639385-45642487 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I045136 | chr19 | 45639563 | 45641967 |
|
Enhancer Sequence | TCCCCTCAAG TTCGTGGGCC CTTTGGGGGT CAAATGGTTA AGACCAGGGC ATGCATGGGC 60
TTGTCCATGG CTTGGGGTAG CTGCTGCAGT CCTGGGGGCT GCCTTCCCAG GCAGGGCAAG 120
CTCCGGTCCC CACTAGAGCT CCAGGGTCAC CAAGCACATG GGCCTTTGTC AGACAGCTCC 180
CTTTCTGTCT GCAAGAGGGG CACCTGCCAT CAGCTGATCC CCTGCAGCTC CTCCCAGGCC 240
TCCACCCCCA AGGAGGAGGA AGTGCTCAGG CAGGGACCAG GCCTGACCTC TGGGGAGGCT 300
GGCGGCTGGC CTCTGTCGGC TTCTTTCCTC CAGCACCGCA GTTCAGCAAC CCACCGCCAC 360
CCAGCACAGT GGCCAGAGCG GAGTCCCAGG GTCTGATGTT AGACTCTGCT CTGGACCAGC 420
CACCTGGTCC CAGGGAGACA CCATACTTTA CCCAGACCTC AGCTTCTTCC CCTAGAAAAT 480
GGGGCAGTGC TTGATGAGAC CAGGGGTCCA GAGCCCCTGG CCTAGCAGGG TGGCAGGAGG 540
AGGAGTCCAC ACGGAGATAT TACTGGACTG GGAGCTCTCT CAGGGACTCC CACTGCGTCC 600
AGCAGCAGCG GATTGGCAGC AGGGCGAGGG GCCCCCCCCC CAAGAAGCTG CCAGCAAGCC 660
CTCTTCCTGG CCCCCTTCCC TGCCCATTGT GGCATCTCCA TGCCCAATAT CTGCTGGCCC 720
GAAGATCTTT CTAACGGCCA GTCCTGACCT CTCCCTCTTC TGCTCCTAGC CTTTCCTTCC 780
TGCTCCGCTG GTCACCCTGA GGTAAAATCC AAGCTCTAAT AGCCAAAAAC TGGAAACAGT 840
ACAAATTCCT GTCAGCTGGT GAATGGGCAA ACACAACGCA GCACATCCTA TAATTACTCT 900
TCAGCAGTAT AAAGGGACTG AAACTCACGC TCATTATGCT CAGTAAGAGA AGCCAACCGC 960
AGAAGGCCAC ACAGTTTCAA TTCCATTTTA ATGAAATGTC CAGAAAAGGC AAATCTGTGT 1020
AGATAGAAAG CCCAGCCCTC CCTTCCGCAT GGTGGCGGCT GTGGCCCTCC AGGGACCGGG 1080
GCTGCAGCTG TTGGGTTTGG GCTACGTCCC TTCATTCATG CTGGGAGCCA CTGCCTGTTA 1140
GCCTGGGAAC ACCCGGGACC AGGCCTGTCT CTTCCAACTG CTTCTGTGTC CTGCGTCAAG 1200
GGGCCGGGCC CTGAATAGCG TACGGCGATG TTTAGCTGTT GAGAGTGTTT TGGGAGTGGG 1260
GATCCTGAGA GGCACGTGGC ATTGTAGTTG AGAGCTGAGT TCAAAGCCCG GCTCGCATAT 1320
ATACCAGGTG TGTGATCTTG GGCAAGGTTG TTTCTCTGAG CTTGGTTTCC TCATAGGGTT 1380
GAAGTGAGGA TTCATTCTTT CACCCAAAAA TACAAAAATA CAAAAAAAAA AAAAACAAAC 1440
CAAGGACCAA GTACAGTGGC TCATACCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCAGA 1500
AGGATTGCTG AAGCCCAGGA GTTCGAGACC AGCCTGGGCA ACATAGTGAC ACCCCATCTC 1560
CACCAGAAAT AAAAATGATC TGGGCGTGAC AGTGCAAGCG TTTGGTCTCT GCTGCTCGGG 1620
AGGATGCTTG AGCCTGGGAG GTCAAGGCTG CAGTGAGCCA TGTTCTCACC ACTTTACTTC 1680
AGCCTGAGCA 1690
|
